Canonical Allele Identifier: CA392320158

Gene: FBN1

Linked Data

• gnomAD v4: 15-48411361-C-T
• MyVariant Identifiers: chr15:g.48703558C>T (hg19) ; chr15:g.48411361C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48411361C>T , CM000677.2:g.48411361C>T	GRCh38
NC_000015.9:g.48703558C>T , CM000677.1:g.48703558C>T	GRCh37
NC_000015.8:g.46490850C>T	NCBI36
NG_008805.2:g.239428G>A , LRG_778:g.239428G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000559133.6:c.*1053G>A	ENSP00000453958.2:n.*1053G>A
ENST00000674301.2:c.*1758G>A	ENSP00000501333.2:n.*1758G>A
ENST00000682158.1:n.1626G>A
ENST00000682170.1:n.2426G>A
ENST00000682767.1:n.1542G>A
ENST00000316623.10:c.8245G>A MANE Select	ENSP00000325527.5:p.Ala2749Thr
ENST00000674301.1:c.3411G>A	ENSP00000501333.1:n.3411G>A
ENST00000316623.9:c.8245G>A	ENSP00000325527.5:p.Ala2749Thr
ENST00000559133.5:c.3614G>A
ENST00000561429.1:n.500G>A
NM_000138.4:c.8245G>A , LRG_778t1:c.8245G>A	NP_000129.3:p.Ala2749Thr
NM_000138.5:c.8245G>A MANE Select	NP_000129.3:p.Ala2749Thr